Product code JAY— Anesthesiology

ADJUSTABLE TUBE TREE FOR ANESTH. HOSES

Classification name
Support, Breathing Tube
Device class
Class 1
Regulation
21 CFR 868.5280
Advisory panel
Anesthesiology
Total cleared
19
First cleared
Most recent

Market context for product code JAY

FDA has cleared 19 devices under product code JAY between 1977 and 1995, filed by 14 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

Top applicants under product code JAY

Recent clearances under product code JAY

Data sourced from openFDA. This site is unofficial and independent of the FDA.